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Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition
The primary motor cortex (M1) exhibits a protracted period of development, including the development of a sensory representation long before motor outflow emerges. In rats, this representation is present by postnatal day (P) 8, when M1 activity is “discontinuous.” Here, we ask how the representation...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591925/ https://www.ncbi.nlm.nih.gov/pubmed/37690023 http://dx.doi.org/10.1016/j.celrep.2023.113119 |
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author | Glanz, Ryan M. Sokoloff, Greta Blumberg, Mark S. |
author_facet | Glanz, Ryan M. Sokoloff, Greta Blumberg, Mark S. |
author_sort | Glanz, Ryan M. |
collection | PubMed |
description | The primary motor cortex (M1) exhibits a protracted period of development, including the development of a sensory representation long before motor outflow emerges. In rats, this representation is present by postnatal day (P) 8, when M1 activity is “discontinuous.” Here, we ask how the representation changes upon the transition to “continuous” activity at P12. We use neural decoding to predict forelimb movements from M1 activity and show that a linear decoder effectively predicts limb movements at P8 but not at P12; instead, a nonlinear decoder better predicts limb movements at P12. The altered decoder performance reflects increased complexity and uniqueness of kinematic information in M1. We next show that M1’s representation at P12 is more susceptible to “lesioning” of inputs and “transplanting” of M1’s encoding scheme from one pup to another. Thus, the emergence of continuous M1 activity signals the developmental onset of more complex, informationally sparse, and individualized sensory representations. |
format | Online Article Text |
id | pubmed-10591925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105919252023-10-23 Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition Glanz, Ryan M. Sokoloff, Greta Blumberg, Mark S. Cell Rep Article The primary motor cortex (M1) exhibits a protracted period of development, including the development of a sensory representation long before motor outflow emerges. In rats, this representation is present by postnatal day (P) 8, when M1 activity is “discontinuous.” Here, we ask how the representation changes upon the transition to “continuous” activity at P12. We use neural decoding to predict forelimb movements from M1 activity and show that a linear decoder effectively predicts limb movements at P8 but not at P12; instead, a nonlinear decoder better predicts limb movements at P12. The altered decoder performance reflects increased complexity and uniqueness of kinematic information in M1. We next show that M1’s representation at P12 is more susceptible to “lesioning” of inputs and “transplanting” of M1’s encoding scheme from one pup to another. Thus, the emergence of continuous M1 activity signals the developmental onset of more complex, informationally sparse, and individualized sensory representations. 2023-09-26 2023-09-09 /pmc/articles/PMC10591925/ /pubmed/37690023 http://dx.doi.org/10.1016/j.celrep.2023.113119 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Glanz, Ryan M. Sokoloff, Greta Blumberg, Mark S. Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title | Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title_full | Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title_fullStr | Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title_full_unstemmed | Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title_short | Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
title_sort | neural decoding reveals specialized kinematic tuning after an abrupt cortical transition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591925/ https://www.ncbi.nlm.nih.gov/pubmed/37690023 http://dx.doi.org/10.1016/j.celrep.2023.113119 |
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